About this role
About the Role Join ICON as a Clinical Research Associate II focused on early-stage development (non-oncology) in the West Region. You will design and analyze clinical trials, interpret complex medical data, and help advance innovative therapies through rigorous monitoring and collaboration with investigators. What You'll Do
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports What We're Looking For
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- At least 2 years Phase I experience as a CRA within any therapeutic area
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel as required (approximately 65-75%)
- West region experience or intent to work in West Region Compensation & Benefits
- Salary range: USD 91,336.00 - 114,170.00 per year
- Bonus, commission, stock, and benefits as described in the posting
- Benefits examples include annual leave, health insurance, retirement planning, LifeWorks EAP, life assurance, and flexible country-specific benefits